Unbounded boundaries and shifting baselines:...
Transcript of Unbounded boundaries and shifting baselines:...
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Unbounded boundaries and shifting baselines: estuaries and coastal seas in a rapidly changing
world
Little, S.1*, Spencer, K. L.2, Schuttelaars, H. M.3, Millward, G. E.4 and Elliott, M.5 1 Nottingham Trent University, School of Animal, Rural and Environmental Sciences, Brackenhurst,
Southwell, Nottinghamshire NG25 0QF. 2 Queen Mary University of London, School of Geography, Mile End Road, London E1 4NS. 3 Delft Institute of Applied Mathematics, Delft University of Technology, Mekelweg 4, 2628 CD Delft,
The Netherlands 4 Plymouth University, Faculty of Science and Environment, Marine Building, Drake Circus, Plymouth,
Devon, PL4 8AA 5 Institute of Estuarine and Coastal Studies, University of Hull, Hull, HU6 7RX, UK.
*Corresponding author: [email protected], +44(0)115 848 5278.
Abstract
This Special Issue of Estuarine, Coastal and Shelf Science presents contributions from ECSA 55; an
international symposium organised by the Estuarine and Coastal Sciences Association (ECSA) and
Elsevier on the broad theme of estuaries and coastal seas in times of intense change. The objectives
of the SI are to synthesise, hypothesise and illustrate the impacts of global change on estuaries and
coastal seas through learning lessons from the past, discussing the current and forecasting for the
future. It is highlighted here that establishing impacts and assigning cause to the many pressures of
global change is and will continue to be a formidable challenge in estuaries and coastal seas, due in
part to: (1) their complexity and unbounded nature; (2) difficulties distinguishing between human-
induced changes and natural variations and; (3) multiple pressures and effects. The contributing
authors have explored a number of these issues over a range of disciplines. The complexity and
connectivity of estuaries and coastal seas have been investigated through studies of physicochemical
and ecological components, whilst the human imprint on the environment has been identified
through a series of predictive, contemporary, historical and palaeo approaches. The impact of
human activities has been shown to occur over a range of spatial and temporal scales, requiring the
development of integrated management approaches. These 30 articles provide an important
contribution to our understanding and assessment of the impacts of global change. The authors
highlight methods for essential management/mitigation of the consequences of global change and
provide a set of directions, ideas and observations for future work. These include the need to
consider: (1) the cumulative, synergistic and antagonistic effects of multiple pressures; (2) the
importance of unbounded boundaries and connectivity across the aquatic continuum; (3) the value
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of combining cross-disciplinary palaeo, contemporary and future modelling studies and; (4) the
importance of shifting baselines on ecosystem functioning and the future provision of ecosystem
services.
Keywords: estuaries, coasts, coastal seas, global change, environmental change, climate change,
Anthropocene
1. Introduction
Since the beginning of the 20th Century, human population growth and activities have exerted
significant pressures on natural systems, which has led to anthropogenic-driven environmental
change on a global scale (Meybeck and Vörösmarty, 2005, Waters et al., 2016, Rockstrom et al.,
2009). These pressures include: (1) modification of the atmosphere and the climate through
increasing greenhouse gas (GHG) emissions; (2) degradation and destruction of habitats (e.g. urban
and agricultural expansion and seabed modification); (3) over-exploitation of resources (e.g. hunting,
fishing and harvesting); (4) modification of the hydrological cycle (e.g. river-diversion, dam
construction and freshwater abstraction); (5) introduction of invasive species; and (6) release of
contaminants into the environment (from fossil fuel combustion, fertiliser applications, intensive
agriculture, changing sediment yields and aquaculture) (Parmesan et al., 2013, Rockstrom et al.,
2009). These pressures do not occur in isolation, they are linked and interact, leading to cumulative,
synergistic and antagonistic effects on natural systems over a range of spatial and temporal scales
(Steffen et al., 2007, Lotze et al., 2006, Scavia et al., 2002, Brown et al., 2013).
Global change is occurring rapidly (Waters et al., 2016, Rockstrom et al., 2009). In the last 50 years,
world population has grown rapidly (from 2.5 billion in 1950 to 7.6 billion in 2017; United Nations,
2017) and the world’s ecosystems have changed more extensively than in any other period in human
history (Pimm et al., 1995, Ceballos et al., 2017). The Earth is currently experiencing a period of mass
global species extinction (the sixth great extinction event; Ceballos et al., 2017), and atmospheric
concentrations of GHG’s have substantially increased (e.g. atmospheric CO2 concentration has risen
from 310 to 407 ppm since 1950; Scripps Institution of Oceanography, 2017) resulting in a rapid
global warming (IPCC, 2013). Since 2010, new global record temperatures have been set in 2014,
2015 and 2016 (Hughes et al., 2017a). This rapid rate of change and the resultant impact on
ecosystems has increasingly become an issue of global concern and has led to the proposal of a new
geo-stratigraphic Epoch, where humans have become a global factor affecting ecosystems; the
Anthropocene (Waters et al., 2016, Steffen et al., 2011).
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All ecosystems are affected by human pressures; however, estuaries and coastal seas carry a
disproportionate human load (Birch et al., 2015, Neumann et al., 2015). Globally, more than 600
million people live in low-lying coastal regions (between 0-10 m above sea level; McGranahan et al.,
2007), with more than 150 million people living within 1 m of high tide (Lichter et al., 2010). Many of
these are concentrated in urban agglomerations, where population density continues to increase
(between 1950 and 2000 the percentage of the world’s population living in urban areas grew from
30 to 50%; Neumann et al., 2015, Steffen et al., 2007, McGranahan et al., 2007). In 2009 67% of the
world’s megacities (cities with more than 10 million inhabitants) were located on the coast, with an
additional 80% having a coastal influence (von Glasow et al., 2013). Urbanisation and increased
anthropogenic activity both on the coast and within catchments (e.g. aquaculture, fisheries,
agriculture and land-use change) have resulted in habitat loss and modification and the release of
contaminants, sediments and nutrients into estuarine and coastal systems (Meybeck and
Vörösmarty, 2005, Sinha et al., 2017). These pressures look set to increase, as by 2025, the
population in coastal zone megacities is projected to reach 301.7 million people (von Glasow et al.,
2013).
In addition to this rapid anthropisation of the coastal zone, global climate change, and its associated
effects, pose further threat to coastal seas and estuarine ecosystems (IPCC, 2014). Whilst the specific
impacts of climate change will vary geographically (based on regional contexts and the physical and
geological setting; Perillo and Piccolo, 2011), coastal and estuarine systems around the world are
becoming increasingly vulnerable to global sea level rise, increased temperatures, ocean
acidification, changes in wind patterns and storminess and changes in the availability of water and
nutrients from precipitation and runoff from land (Day et al., 2011; IPCC, 2014). Likely consequences
of these changes include habitat loss through coastal erosion, coastal squeeze and marine
transgression (Gutierrez et al., 2011, Jackson and McIlvenny, 2011), enhanced risk of coastal
eutrophication, harmful algal blooms and hypoxia (Sinha et al., 2017), reductions in water clarity
(Capuzzo et al., 2015), landward incursion of saltwater into estuaries (Little et al., 2016) (and coastal
groundwater aquifers; Ferguson and Gleeson, 2012) and corresponding movement of the turbidity
maxima (Jalon-Rojas et al., 2015). The resulting impacts of these changes on ecology and
biogeochemical cycling have consequences for the structure and functioning of estuaries and coastal
seas (Hughes et al., 2017b, Elliott et al., 2015, Richardson et al., 2012).
Whilst we do not yet fully understand to what extent global change will affect estuarine and coastal
processes (Richardson et al., 2012), it is clear that these systems face unprecedented pressures,
which will affect human societies through the loss of the ecosystem services they provide (e.g.
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provisioning services such as food, fuel and fibre; regulating services such as nutrient cycling,
atmospheric and climate regulation, waste processing, disease regulation and flood hazard
regulation; and cultural services such as tourism, education, recreation, amenity and aesthetical
values; MEA, 2005, Barbier et al., 2011). Coastal systems (including estuaries, continental shelf area,
sea grass, coral reefs, mangroves and wetlands) are clearly valuable resources (total economic value
estimated at ∼US$ 575,011 per ha per year at 2007 price levels; de Groot et al., 2012), which face
competing and often conflicting socio-economic and environmental demands. They are also complex
systems, connected and naturally variable, governed by interacting geomorphological, hydrological
and ecological processes acting at a range of temporal and spatial scales (Elliott and Whitfield, 2011,
Whitfield and Elliott, 2011). The need to balance these socio-economic and environmental demands
in a complex environment, whilst confronting the consequences of global change requires innovative
multi-sectoral management approaches based on excellent and fit-for purpose multi-disciplinary
science (Elliott and Whitfield, 2011).
With this objective in mind, the Estuarine and Coastal Sciences Association (ECSA) and the publisher
Elsevier organised the 55th ECSA international symposium in London, UK on the 6th of September
2015. This multi-disciplinary symposium brought together 363 researchers and professionals from
223 institutions and 36 countries to discuss and address issues of outstanding scientific importance
in the science and management of estuaries and coastal seas. The goal of the symposium was to
synthesise knowledge from a variety of disciplines to stimulate future multi-disciplinary research and
aid global environmental management of these systems in the face of multiple pressures (as
outlined above). This Special Issue consists of 30 individual papers which are discussed in relation to
main focus of the symposia; learning lessons from the past, discussing the current and forecasting
for the future, addressing the impacts of global environmental change on estuaries and coastal seas
across the globe.
2. Overview of the problem
The theme of the meeting and this Special Issue (SI) is based on a consensus that estuaries and
coastal seas are changing, threatened and in a state of global decline due to multiple drivers
resulting in interacting pressures which act over a number of spatial and temporal scales. These
include the effects of global climate change (e.g. global sea level rise, increasing temperatures and
ocean acidification; IPCC, 2014) and other human activities (e.g. invasive species, over-extraction of
resources, habitat loss and alteration, introduction of organics, nutrients, pollutants and
contaminants, marine litter and changes to water flow; Syvitski et al., 2005, Lotze et al., 2006). These
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pressures have been linked to the depletion of > 90% of formally important estuarine and coastal
species (i.e. large vertebrates and habitat-providing species; Lotze et al., 2005), the loss of > 65% of
coastal vegetated ecosystems (Lotze et al., 2006, Polidoro et al., 2010), water quality degradation
(nutrient input into the oceans has trebled since 1970; Smith et al., 2003) and accelerated species
invasions (Ruiz et al., 1997).
Estuaries are particularly vulnerable to these pressures as they are ‘open’ ecosystems with ill-
defined and changing unbounded boundaries (Elliott et al., 2015). Estuaries are both connected to
and part of a dynamic aquatic continuum, linking the terrestrial environment (through streams,
rivers and run-off) with the continental shelf and open ocean (Elliott et al., 2015). Energy, organisms
and matter flow within, through and between these unbounded systems (Hyndes et al., 2014), so
pressures acting on a range of spatial (e.g. local, regional and global) and temporal (i.e. days, months
and decades) scales converge and impact on estuaries (i.e. endogenic pressures emanating from
within the system and exogenic pressures emanating from outside the system) (Raimonet and
Cloern, 2017, Elliott, 2011). As a result, estuarine baselines are shifting. Marine transgression and
saline incursion from global sea level rise are increasing the extent of marine influence inland (Little
et al., 2016). Habitat loss and reclamation (e.g. managed realignment) are altering the morphology
of the coastline, through changes to sediment erosion and deposition processes (Cazenave and
Cozannet, 2014). Increased suspended sediments in the water column (through increased coastal
erosion, decreased estuarine sediment sinks and changing weather patterns) are reducing water
clarity in coastal seas, changing energy fluxes through the marine food web (Capuzzo et al., 2015).
Increased temperatures and species introductions are resulting in species redistribution, turnover
and range shifts, with consequences for functional biodiversity (Johnson et al., 2011, Lotze et al.,
2006, Walther et al., 2009, Graham et al., 2014). Increasing chemical, organic and microbial pollution
of coastal waters and sediments are leading to changing timings and extents of algal blooms and
hypoxic zones (Sheahan et al., 2013).
These unbounded boundaries and shifting baselines have resulted and continue to result in changes
to ecosystem structure and functioning and our ability to monitor, assess and manage these systems
in order to ensure continued provision of ecosystem services in to the future. In addition, these
changes will impact upon the ability to comply with environmental legislation (e.g. the use of
baselines/reference/threshold values to assess Good Environmental and Ecological Status (as per the
Marine Strategy Framework Directive and Water Framework Directive respectively; Elliott et al.,
2015).
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One of the most prominent and challenging issues facing researchers and professionals in the field is
that in order to predict, manage and mitigate the impact of global change in a complex unbounded
environment, we need to understand: (1) the natural variability and interacting processes occurring
within and between these systems; and (2) how the system responds to endogenic managed and
exogenic unmanaged pressures and their interacting effects. With a solid understanding of the
structure and functioning and natural variability of these systems (both before and during human
influence), we can then (3) forecast for different future scenarios with greater confidence. In such
complex systems, this requires a holistic approach which reaches across traditional disciplinary
divides (e.g. physical, chemical and ecological; palaeo, contemporary and theoretical). We can then
(4) propose appropriate adaptive management approaches based on a strong scientific foundation
in collaboration with policy makers and stakeholders.
2.1 Learning lessons from the past
Humans have altered and manipulated estuarine and coastal systems for thousands of years
(Weckström et al., 2017, Canuel et al., 2017, Long et al., 1998, Taffs et al., 2008) making it difficult to
isolate anthropogenic from environmental influences and identify reference (or ‘baseline’)
conditions for contemporary and future modelling studies (Lotze et al., 2006, Bentley et al.,
2017). Studies that apply a long-term perspective are key here, as they can indicate trajectories of
change both before and during human occupation that more traditional contemporary studies
cannot (e.g. preceding the instrumental record). This is valuable in determining the degree of
anthropogenic influence in estuarine and coastal areas (i.e. fluctuation from this baseline),
understanding natural variability of the system and for contextualising present-day trends and
ecosystem functioning in the longer-term, all of which are essential for successful coastal
management and restoration (Bennion and Battarbee, 2007, Santschi et al., 2001, Bentley et al.,
2017). In this SI, a number of authors applied palaeoecological or historical approaches to evaluate
human imprint and gain a pre-industrial perspective on estuarine status.
Using sedimentological and diatom evidence, Andrén et al. (2016) reconstructed the history of
eutrophication and quantified total nitrogen (TN) concentrations for the Gårdsfjärden estuary in the
central Bothinia Sea. The imprint of anthropogenic activity was recorded from 1920, when
discharges of industrial point source pollution resulted in hypoxic bottom waters. Good ecological
status was recorded prior to this point and TN reference conditions for the estuary were successfully
determined.
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Álvarez-Vázquez et al. (2016) and Bojórquez-Sánchez et al. (2017) investigated trace element
enrichment in estuarine and lagoon sediments in order to evaluate the impact of human activities
over time. Álvarez-Vázquez et al. (2016) investigated the lithogenic imprint of trace metals in the
Galician Rias (NW of the Iberian Peninsula) during the Anthropocene. Slight human impact was
observed from the mid-20th century linked to river damming, bridge/road constructions and
changes in catchment land use. The pre-industrial record showed lithogenic differences in the
drainage basin, highlighting the importance of using local background references in contamination
studies. Bojórquez-Sánchez et al. (2017) investigated trace element enrichment in the Salada coastal
lagoon in Veracruz (Mexico), which receives cooling water discharge from the Languna Verde
Nuclear Power Plant. Sediments (dated from 1900-2013) were enriched in silver (Ag), arsenic (As)
and chromium (Cr) which corresponded to the geology of the coastal zone and local mining activity.
The profiles of the element fluxes reflected the construction (1970s) and operation of the power
plant; however, no evidence of pollution was detected.
Donnici et al. (2017) employed a palaeo-approach to investigate the sedimentation rate and lateral
migration of tidal channels in the Lagoon of Venice (Northern Italy) over the Holocene (past 5,000
years). Buried tidal channels were identified and mapped and compared with historical and current
maps, revealing human intervention on some of the tidal channels (i.e. simplified morphology) and a
general reduction in the number of channels over time. The importance of understanding the
natural morphological evolution of these environments before implementing artificial interventions
was highlighted. Liu et al. (2016) employed historical bathymetric data to investigate the
morphological evolution of Jinshan Trough in Hangzhou Bay (China) from 1960-2011. Whilst complex
and driven by multiple factors, Liu et al. (2016) postulated that human activities (i.e. coastal
reclamation) and climate (i.e. storm surges) were likely two of the main influencing factors on
morphological change, through changes to erosion and deposition processes.
2.2 Discussing the current
2.2.1. Unbounded boundaries and the importance of scale
The connectivity of estuaries to marine and freshwater sources is widely accepted as being integral
to the structure and functioning of estuarine and coastal ecosystems (Elliott and Whitfield, 2011,
Gillanders et al., 2011). Despite this, we do not fully understand the importance of this connectivity
on ecosystem health and resilience (Raimonet and Cloern, 2017, Hyndes et al., 2014). In this SI,
Wolanski (2016) and Qian et al. (2016) explored the importance of these unbounded boundaries and
scale for coastal flora and fauna and the development of hypoxic zones.
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Wolanski (2016) investigated the importance of unbounded boundaries for self-recruitment and
connectivity for a range of estuarine and coastal fauna and flora from a number of case study areas.
By integrating physical oceanographic observations and modelling with studies of species behaviour,
tracking and population dynamics, Wolanski determined that the spatial scales for self-recruitment
and connectivity vary between species from a few metres to 10, 000 km and temporal scales vary
from one to three generations. Wollanski (2016) identified that these unbounded boundaries,
together with the hydrology and ecological dynamics of particular species, was key in creating the
“functional connectivity between parts of the aquatic continuum from the river catchment to the
open seas”.
Qian et al. (2016) also noted the importance of scale and connectivity in understanding the impact
of non-local drivers of summer hypoxia in the East China Sea off the Changjiang (Yangtze River)
Estuary; one of the largest coastal oxygen-depleted areas in the world. Qian et al. (2016) identified
that the formation and maintenance of the hypoxic conditions in the East China Sea were related to
the initial dissolved oxygen (DO) level of the source water masses, the biogeochemical alterations of
the water mass mixture during travel and the evolution of DO on the pathway to the hypoxic zone.
The source water masses mixed ~1300 km upstream and travelled ~60 days to reach the of the
hypoxic zone. Qian et al. (2016) argued that far field drivers should be taken into account in order to
better predict the future scenarios of coastal hypoxias in the context of global warming.
2.2.2. Biology and ecology
Human activities are resulting in widespread and unprecedented biodiversity loss and turnover (β-
diversity scale) in many biological components (Ceballos et al., 2017, Pandolfi and Lovelock, 2014).
Such changes have potential implications for the provision of ecosystem services, based on the role
of biodiversity in ecosystem functioning (Naeem et al., 2012). This role is subject to much debate
(i.e. the Biodiversity Ecosystem Function (BEF) debate; Strong et al., 2015), however over the last
decade, functional diversity (measured by the value and range of the functional traits of an organism
present in a community) has increasingly been used over (or in addition to) traditional structural
assessments of biodiversity (i.e. species taxonomic diversity, abundance and biomass) to assess and
manage the impact of human pressures on estuarine and coastal systems (Dolbeth et al., 2016,
Covich et al., 2004). This is because these trait-based approaches can provide information on
multiple aspects of ecosystem function and as such detect anthropogenic stress (Dolbeth et al.,
2016), which is often not visible using a structural approach (i.e. the Estuarine Quality Paradox;
Elliott and Quintino, 2007).
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Helenius et al. (2016) applied a functional trait-based approach to investigate the drivers of littoral
zooplankton community distribution and spatial heterogeneity in a shallow coastal area of the
northern Baltic Sea (southwest Finland). Salinity and to a lesser extent turbidity and temperature
were found to be the main predictors of the spatial patterns and functional diversity of the
zooplankton community. Therefore, this study provides important baseline information, essential to
assessing the impacts of eutrophication and temperature rise on plankton communities in brackish
coastal areas with narrow salinity gradients.
Silva-Júnior et al. (2016) employed a traits-based approach (food acquisition and locomotion) to
quantify the functional diversity of fish in four tropical estuaries in northeast Brazil, subject to
different levels of human impact (e.g. mangrove deforestation, shrimp farming, fishing etc.) and
environmental conditions. Silva-Júnior et al. (2016) determined the functional typology of fish
assemblages per estuary by combining fish abundance and functional dissimilarities data into a
multivariate analysis. The species contribution in functional typology could therefore be assessed
and the diversity assessment of estuarine fishes improved, and may be an important tool in
estuaries faced with perturbations. Differences between estuaries were identified based on the
functional typology and attributed to marine influenced hydrological features, similar levels of
species abundances and morphological traits.
Mancinelli et al. (2017) investigated the trophic role and feeding flexibility of the invasive Atlantic
blue crab (Callinectes sapidus) in the Mediterranean Sea. The authors observed that C. sapidus had
a high trophic flexibility expressed at both an inter- and intra- population scale and postulated that
this trophic generalism is likely linked to their invasion and establishment success. Callinectes
sapidus is one of 106 alien marine crustacean species recorded in the Mediterranean Sea, many of
which have become established (Galil, 2011). These invasive crustaceans have had profound
ecological impacts through changes to the community composition and biodiversity loss of native
marine species (Galil, 2011).
Habitat restoration on estuaries and coasts is a key approach to restoring habitats detrimentally
impacted and/or lost through human activities (Elliott et al., 2007). Replicating the structure and
function of natural habitats in the restored sites has, however, proven difficult (Mossman et al.,
2012, Elliott et al., 2007). Barnuevo et al. (2017) reviewed the practice of large-scale monospecific
mangrove plantations in the Philippines in order to assess whether restoration measures were able
to reproduce the structure and functioning of natural mangrove forests. Barnuevo et al. (2017)
found that even after 60 years of establishment, the structural development and complexity of the
planted forests were lower than the reference natural forests, but inter-site differences were
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observed. Secondary succession was inhibited in a densely planted monospecific plantation
(reflected by a low regeneration potential), whereas recruitment and colonisation of non-planted
species were promoted in a secondary site. The authors identified the importance of reviewing
current reforestation practices in order to focus on restoring the characteristics and functioning of
natural mangroves, rather than solely focussing on the socio-economic benefits (e.g. fuelwood,
timber and coastal protection). The importance of this was highlighted by Abdullah and Lee (2016),
who observed that the complex dynamic habitats and the spatial heterogeneity of natural mangrove
environments played an important role in the spatio-temporal structure of meiofaunal assemblages
in eastern Australia. Meiofauna significantly contribute to ecosystem functioning in soft-sediment
ecosystems (Nascimento et al., 2012) and were recorded in highest densities in sediments where
food proxies were in high availability and habitat structure provided the best conditions.
2.2.3. Pollution and contamination
Increased inputs of sediment, pollutants and contaminants (e.g. organic matter, inorganic nutrients,
metals and organic chemicals) are major threats to the health of global estuaries and coasts (Dachs
and Méjanelle, 2010). The causes are wide-ranging, but most often linked to urbanisation of the
coastal zone and development of catchments for urban, industrial and intensive agricultural uses
(Sutherland et al., 2016, Sharley et al., 2016). Coastal and estuarine waters receive contaminants,
both via the catchment (e.g. riverine inputs; Sharley et al., 2016) and local anthropogenic activities
via point and diffuse sources (Jeffries et al., 2016, Eggleton and Thomas, 2004). Many of these
contaminants accumulate in estuarine sediment (through binding with particulate matter and
settling) and become part of the water-sediment system (Koukina et al., 2016). At high
concentrations, these contaminants can have toxic or enriching effects on biota and interfere with
important ecosystem functions (e.g. fluxes of energy or material through productivity,
decomposition and nutrient cycling). In this SI, a number of contributors investigated the sources
and distribution of metals in estuarine and marine sediments.
Koukina et al. (2016) demonstrated that both natural (e.g. turbidites) and human pressures (e.g.
urban and industrial activities) influence the abundance and speciation of potential contaminants
(and therefore change their bioavailability) in the Cai River estuary and Nha Trang Bay in the South
China Sea, Vietnam. Marmolejo-Rodríguez et al. (2016) investigated geochemical associations and
anthropogenic influences of major and trace elements in the Central Pacific Mexican Shelf (CPMS);
an area influenced by natural (e.g. storms and hurricanes) and anthropogenic pressures (industrial
coastal areas, farming, fishing and agriculture). An anthropogenic influence was detected for
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mercury (Hg) and silver (Au) in the CPMS near the heavily industrialised harbour of Lazaro Cardenas,
which has implications for biota through their high toxicity in marine waters.
Zaborska et al. (2016) investigated the distribution of heavy metals and 137Cs in the central part of
the Polish maritime zone, to assess the potential impact of contaminant re-suspension during
construction and functioning of a proposed wind farm development. Within the 9000 km2 study area
of the Polish economic zone, the deepest regions (e.g. Slupsk Furrow and Bornholm Basin) were
found to contain the largest contamination by heavy metals. Deeper areas have been recorded as
being a sink for heavy metals and radionuclides, as they are characterised by fine-grained sediments,
which heavy metals attach to. The shallow (20-40m) sandy sediments of the Southern Baltic were
characterised by the lowest concentration of heavy metals (often below natural environmental
background) and are therefore appropriate for offshore wind energy construction.
Fialkowski and Rainbow (2016) used the amphipod crustacean Talitrus saltator to investigate the
spatial distributions of trace metal bioavailabilities in Baltic Sea coastal waters. Variations in the
geographical distributions of metal bioavailabilities were observed, with western regions of the
Baltic experiencing higher bioavailabilities than the eastern region. The regions influenced by the
Oder and Vistula rivers had noticeable differences in metal bioavailabilities.
A number of contributors investigated the sources and impact of organic matter and contaminant
discharge on benthic sediment biogeochemical processes. Wang et al. (2016) observed that in the
northern Taiwan Strait, settling particulate organic matter (POM) was primarily from marine sources
and the re-suspension of bottom sediment by currents. Sutherland et al. (2016) compared the
impact of urban storm drain organic matter and contaminant discharge on benthic sediment
biogeochemical processes in high and low flow systems (i.e. a highly flushed channel and poorly
flushed embayment respectively). Increased oxygen consumption from benthic metabolism was
evident closest to poorly flushed discharge points, related to the high retention and accumulation of
organic matter and contaminants in the sediment. Sutherland et al. (2016) stated that monitoring
benthic oxygen fluxes in this way could be a sensitive measure of ecological change in sediments
following large inputs of storm water contaminants (i.e. following high precipitation events).
Global climate change impacts including increasing temperatures and changing precipitation
patterns and storminess may play a significant role in organic matter degradation in estuarine
sediments. Vincent et al. (2017) found that higher heterotrophic microbial activity appeared to be
favoured by higher temperatures in the Ashtamudi estuary in Kerala, India. In addition, the
contribution of organic matter and nutrient deposition to estuarine sediment via urban run-off
during the monsoon season, resulted in a two-fold and five-fold increase in methanogenesis and
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denitrification respectively, increasing the production of the greenhouse gases nitrous oxide (N2O)
and methane (CH4). Canu and Rosati (2016) modelled the long-term (100 yrs) dynamics of the
mercury cycle in the Marano-Grado Lagoon (a Mediterranean mercury hotspot), and showed that a
sea level rise (of 0.315 m) and temperature rise (+2.5°C) may increase sediment methylmercury
(MeHg) by up to 87% and 95% of current levels. Mercury bioaccumulation in biota was projected to
increase accordingly.
2.2.4 Sediment dynamics
Human activities (e.g. port developments, dredging, management of intertidal areas, deforestation
and freshwater abstraction) and climate change (e.g. global sea level rise, drought, changes to wind
and precipitation patterns and storminess) can modify processes controlling sediment erosion,
transport and deposition; increasing suspended sediment loads in estuaries and coastal seas
(Capuzzo et al., 2015, de Jonge et al., 2014, Syvitski et al., 2005). In this SI, a number of contributors
investigated the physical processes that govern the transport and behaviour of fine sediments in
estuaries.
Jalón-Rojas et al. (2017) employed a combined spectral analyses approach to investigate the relative
contribution of environmental forcing frequencies on turbidity variability in the Gironde and Loire
estuaries in west France. The main environmental factors affecting turbidity were related to river
flow, including hydrological regime and discharge variability, tidal range, tidal cycles and turbulence.
The relative influences of these forcings on turbidity depended on estuarine region (lower or upper
estuary) and the time scale (multi-annual or seasonal). Mitchell et al. (2016) investigated the impact
of different freshwater flow conditions on estuarine turbidity in the tidal reaches of the Kaipara
River, New Zealand. A clear turbidity maximum was observed under low-flow conditions, where fine
sediment was transported landwards and trapped in the upper part of the tidal reach. This turbidity
maximum was flushed downstream under high flows. Sediment suspension was controlled by both
local resuspension of material and by advection of previously suspended material by the main flow.
Braga et al. (2016) employed Landsat 8 satellite images to investigate spatial and temporal variations
of suspended matter patterns and distribution in the Po River prodelta (Italy) from 2013-2015. River
discharge, wind and wave fields, coastal currents and circulation at local and basin scale explained
most of the variability in surface turbidity in the prodelta. Smaller (sub-mesoscale) structures (i.e.
plumes and sand bars) were observed in the near shore environment and were linked to the
interaction between hydro-meteorological factors, coastal currents and prodelta morphology.
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Boudet et al. (2016) and Slinger (2016) modelled sediment transport patterns in the mouth of the
Rhone delta and intermittently open-closed estuaries respectively. Using the Delft3D numerical
model, Boudet et al. (2016) identified that total sediment transport at the Rhone delta outlet was
only influenced by the river flow, whereas at the mouth-bar, total sediment transfer depended on an
equilibrium between the influence of storms and floods and on the succession of these events.
Slinger (2016) developed a model to simulate the opening and closure of the mouths of small, wave-
dominated estuaries characteristic of the coasts of South Africa, Australia, California and Mexico.
Freshwater inflows were shown to be significant in determining the behaviour of the inlet mouth
and the balance between these inflows and wave events were shown to govern the opening/closure
of the mouth of a particular estuary.
2.3 Forecasting for the future
The inherent complexity and unbounded nature of estuarine and coastal systems makes physical
and ecological responses especially challenging to predict. However, our capacity to make
predictions is critical to the success of estuarine and coastal management and conservation in a
rapidly changing world.
2.3.1 Global Sea Level Rise
The Fifth Assessment Report (AR5) of the IPCC projected, with medium confidence, that global mean
sea levels rose by a rate of 3.2 (2.8 to 3.6) mm yr–1 from 1993 to 2010 and are projected to increase
by a further 44-74 cm by 2100 (IPCC, 2013). An alternative estimate which considers the
uncertainties around Greenland and Antarctica ice sheet loss suggest that sea-level could rise by up
to 1.8 m by 2100 (Jevrejeva et al., 2014, Church et al., 2013). In some regions, the addition of
vertical movements of the land (e.g. through glacio-isostatic adjustment, tectonic uplift and
geological subsidence) significantly contribute to changes in sea levels relative to the land (Relative
Sea Level Rise (RSLR); Nicholls and Cazenave, 2010). This acceleration in Global Sea Level Rise (GSLR)
will have a significant impact on estuarine and coastal ecosystems (IPCC, 2014). In this SI, Ciro Aucelli
et al. (2016), Little et al. (2016) and Angus (2016) focussed on evaluating the future effects of RSLR,
through the impacts of marine transgression and saline incursion on estuaries and coasts.
Ciro Aucelli et al. (2016) evaluated the effects of future RSLR on the Volturno River Plain in southern
Italy; a plain characterised by its high economic and ecological value, low topography and severe
land subsidence. Using topographical information and RSLR scenarios, Ciro Aucelli et al. (2016)
determined that the areas prone to inundation would increase by approximately 50% and 60% by
14
the years 2065 and 2100 respectively and would include areas of current infrastructure and
agriculture.
Little et al. (2016) demonstrated that RSLR projections for southeast England will increase estuarine
salinities and drive saline incursion into freshwater tidal areas, which in addition to projected
changes in freshwater river flow, will have important consequences on upper estuarine structure
and functioning. The study identified that the benthic freshwater fauna inhabiting these upper
estuarine zones may demonstrate greater tolerance to salinity change than is currently recognised,
and may persist where salinity increases are gradual and zones unbounded. Angus (2016)
investigated the impacts and challenges of climate change on Scottish saline lagoons and their
specialist lagoon fauna. Rising sea levels are predicted to result in a loss of lagoon habitat through
either marine transgression (through removal of impoundment) and/or increasing salinities. Despite
the wide salinity tolerances of lagoonal species, they may be out-competed by marine species and
their limited dispersal capabilities may restrict their ability to move to compensated lagoon habitats
(i.e. previously freshwater inland water bodies).
In addition to surface saline incursion and marine transgression, seawater intrusion into
groundwater aquifers is predicted to increase with climate change (i.e. RSLR and increased
abstraction of freshwater for irrigation and domestic use). Since the 1970s, over-extraction of fresh
groundwater for agriculture in the Korba coastal plain (northeast Tunisia) has led to seawater
intrusion in the aquifer. In this SI, Slama and Bouhlila (2016) investigated the hydrochemical
processes that occur when freshwater and seawater mix, in order to use these as indicators of
seawater intrusion progression and freshwater flushing into seawater accompanying the discharge
of groundwater to sea (the Submarine Groundwater Discharge). These indicators are important in
order to monitor and assess groundwater saline intrusion progression. Increasing salinization of
coastal aquifers may result in the loss of access to fresh groundwater for more than one billion
people living in coastal regions (Ferguson and Gleeson, 2012).
2.3.2 Integrated management approaches
In this SI, Lillebø et al. (2016) discusses lessons learned from the development of an integrated
management approach of coastal lagoons and their catchments based on scientific strategies and a
decision support framework developed in collaboration with local stakeholders. As part of a
collaborative project, integrated scenarios of possible economic development and environmental
impacts were developed for four European lagoons (Vistula lagoon on the Baltic Sea, Ria de Aveiro
lagoon on the Atlantic Ocean, Tyligulskyi Liman lagoon on the Black Sea and Mar Menor lagoon on
the Mediterranean Sea). These were discussed with local stakeholders, developing specific
15
management recommendations for each study lagoon. These recommendations were translated
into policy guidelines concerning management implementation in a local-regional-European setting.
Lillebø (2016) highlighted the importance of enhancing the connectivity between research and
policymaking in this way and identified a need to better recognise the connectivity between land,
streams, rivers, lagoons and coastal zones. Lillebø (2016) proposed a single coordinating unit for
coastal management on a European scale in view of projected changes in climate and socio-
economic development.
3. Conclusions
The papers presented in this SI have clearly shown that global change is altering the structure and
functioning of our estuaries and coastal seas. However, establishing impacts and assigning cause to
the many pressures of global change is and will continue to be a formidable challenge in these
systems, due in part to: (1) their complexity and unbounded nature; (2) difficulties distinguishing
between human-induced changes and natural variations and; (3) multiple pressures and effects. This
SI has explored a number of these issues over a range of disciplines; contributing to our
understanding and assessment of the impacts of global change, highlighting methods for essential
management/mitigation of the consequences and providing a set of directions, ideas and
observations for future work.
Notably, there is an urgent need to consider the effects of multiple pressures. Studies that
investigate the impact/s of individual pressures on ecosystem structure and functioning provide key
pieces of information for understanding a larger puzzle.However, it is the cumulative, synergistic and
antagonistic effects of multiple pressures (e.g. over-exploitation, habitat loss and climate change
effects) that have been shown to be most significant in the loss, depletion and turnover of species in
estuaries and coastal seas (Lotze et al., 2006, Scavia et al., 2002, Burney and Flannery, 2005, Peer
and Miller, 2014, Bentley et al., 2017). The environmental complexity of estuarine and coastal
systems and the intricacy of underlying drivers means that the effects of multiple pressures (on a
series of ecosystem components and levels of biological organisation; Parmesan et al., 2013) must
be understood in order to assess the overall impacts of global change. Functional group and
ecological network analyses which are interpreted using an integrated approach may prove key here
(Schuckel et al., 2015, Syvitski et al., 2005, Bentley et al., 2017).
The position and role of estuaries within the unbounded aquatic continuum means that exogenic
pressures acting on adjoining ecosystems (terrestrial, freshwater and marine) also act on estuaries.
However, the resultant impacts on estuarine functioning will have reciprocal effects throughout the
aquatic continuum through the loss and alteration of trophic subsidies (i.e. flow and transfer of
16
energy, matter and organisms between ecosystems; the ‘outwelling hypothesis’, Savage et al.,
2012). It is therefore critically important in the face of global change, that we view and manage
these systems as a single continuum. As such, much greater research focus is required on
understanding the importance of this connectivity on the health and resilience of these interlinked
ecosystems (Hyndes et al., 2014).
Research projects which combine palaeo/ historic, contemporary and future modelling approaches
to investigate the effects of multiple pressures on ecosystem functioning at a catchment-scale (i.e.
land, streams, rivers, lagoons and coastal seas) could therefore be a powerful tool to manage and
mitigate global change through adaptive management plans formed in conjunction with local
stakeholders. Just like our unbounded study systems, this requires scientists to reach beyond
traditional discipline boundaries and scales. ECSA international conferences provide this platform,
enabling estuarine and marine researchers and professionals from these different disciplines to
meet, disseminate their research and collaborate through global research networks.
Even with mitigation of the drivers and pressures (exogenic and endogenic) of global change in the
near future, estuarine and coastal baselines will continue to shift. For example, even with the
complete cessation of CO2 emissions by 2100, global climate change has been shown to be
irreversible on centennial to millennial timescales (Katarzyna and Kirsten, 2015). In this scenario,
whilst global mean temperature might remain more constant (Solomon et al., 2009), substantial
regional changes in temperature, precipitation and ocean warming would continue (Gillett et al.,
2011) and thermostatic sea levels would rise for several centuries to come (Katarzyna and Kirsten,
2015). In some systems (e.g. coral reefs; Hughes et al., 2017b), returning to past configurations or
maintaining a current state (i.e. achieving ‘Good Environmental Status’; Elliott et al., 2015), may no
longer be an option and may require radical changes to how we view, manage and govern these
systems (Hughes et al., 2017b). Whilst this SI and most research in this field assesses the threats and
negative impacts of global change on estuaries and coastal seas, such changes could also present
new opportunities. For example, the unbounded boundaries of these systems may result in novel
assemblages and configurations of organisms in the near future, as native species are lost, move or
adapt and joined or replaced by mobile non-natives (due to rising temperatures, ocean acidification
and species introductions; Rius et al., 2014). These new species may, in some cases, support or even
enrich functional biodiversity and as such, play a key role in the maintenance of ecosystem services
(Walther et al., 2009). The global challenge here is to accept and adapt to these changes if mitigation
is untenable, recognising that securing essential ecosystem services into the future will require
scientific developments, innovative technology and adaptive integrated management and
governance of estuaries and coastal seas (Richardson et al., 2012).
17
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